Paving composite and method of paving

ABSTRACT

A tack film material comprises a carrier substrate comprising a polymer film having first and second major surfaces. A surface layer on the first and second major surfaces comprises a resinous non-asphaltic material or a material including about 50% or more resinous non-asphaltic component and about 50% of less of asphaltic component. the surface layer is capable of forming a bond with an adjacent layer of asphaltic paving material, when the surface layer is heated to a temperature of about 120° C. or more under a pressure that is applied to the tack film material by an overlying layer of the asphaltic paving material having a thickness of about 3.8 cm (1.5 inch) or more laid. The surface layer is not tacky at a temperature of about 20° C. and a pressure of about one atmosphere.

FIELD OF THE INVENTION

The present invention relates to reinforcement materials for pavementrepairs.

BACKGROUND OF THE INVENTION

Various methods and composites for reinforcing asphaltic roads andoverlays have been proposed. Some describe fiberglass grids impregnatedwith resins. To repair an old pavement, an asphaltic tack coat isgenerally applied with fiberglass grids according to the constructionregulations. The tack coat is applied as a liquid (for example, as anemulsion or hot asphalt cement binder by spraying), and thereafterchanges from a liquid to a solid. The tack coat is applied on top of theinstalled grid with adhesive coating on the back of the grid, used as anaid in bonding a new asphalt payment to the existing pavement surface.In order to install fiberglass grids without adhesive coating on theback of the grid, the tack coat is firstly applied to an existingpavement. Before the tack coat is fully cured, the grid is laid on thetack coat. As the tack coat cures further, it holds the grid in place onthe underlying pavement. The tack coat partially dissolves and mergeswith the impregnating resin in the grid, when hot asphalt concrete isoverlaid on top of the grid. Tack coats have several highly desirablefeatures for use with such reinforcements. In particular, they arecompletely compatible with the asphaltic concrete or cement to be usedas the overlay, and their fluid nature makes them flow into, and smoothout, rough paving surfaces.

On the other hand, tack coats present several difficulties. Theproperties of tack coats are very sensitive to ambient conditions,particularly temperature, and humidity. These conditions may affect curetemperature of emulsion tack coats, and in severe conditions, they canprevent cure. In less severe circumstances, the overlay paving equipmentmust wait until the tack coat has cured, causing needless delays. Forexample, tack coats are normally emulsions of asphalt in water, oftenstabilized by a surfactant. To manifest their potential, the emulsionmust be broken and water removed to lay down a film of asphalt. Thewater removal process is, essentially, evaporation, which is controlledby time, temperature, and humidity of the environment. Frequently, theenvironmental conditions are unfavorable, resulting in inefficienttacking or unacceptable delay.

JP 05-315732 describes an asphalt film that can be used in place of asprayed emulsion tack coat. The asphalt film is laid over a base layeranD a heated asphalt material is laid on top of the film. The film isformed by attaching asphalt emulsion to both sides of a net-like bodyand solidifying it. A lower base layer comprising gravel, sand, etc. andan upper base layer of crushed stone are placed on a subgrade andcompacted. The film is placed on the upper base layer, and the heatedasphalt material is laid on the film. Additional film and asphaltmaterial layers are repeatedly laid on the asphalt layer. The film issoftened and melted into a single body by the heat of the asphaltmaterial.

Accordingly, there remains a desire to improve the interlaminar layerbetween pavement courses.

SUMMARY

In some embodiments, a tack film material comprises a carrier substratecomprising a polymer film having first and second major surfaces. Asurface layer on the first and second major surfaces comprises aresinous non-asphaltic material or a material including about 50% ormore resinous non-asphaltic component and about 50% or less of asphalticcomponent. The surface layer is capable of forming a bond with anadjacent layer of asphaltic paving material, when the surface layer isheated to a temperature of about 120° C. or more under a pressure thatis applied to the tack film material by an overlying layer of theasphaltic paving material having a thickness of about 3.8 cm (1.5 inch)or more laid. The surface layer is not tacky at a temperature of about20° C. and a pressure of about one atmosphere.

In some embodiments, a method of making a tack film material comprisesproviding a carrier substrate comprising a polymer film having first andsecond major surfaces; and covering the first and second major surfaceswith a resinous non-asphaltic surface layer material or a materialincluding about 50% or more resinous non-asphaltic component and about50% or less of asphaltic component.

BRIEF DESCRIPTION OF THE DRAWINGS

The accompanying drawings illustrate preferred embodiments of theinvention, as well as other information pertinent to the disclosure, inwhich:

FIG. 1 is a partial cross-sectional side view of a repaved section ofasphaltic pavement according to one example;

FIG. 2 is a detailed cross sectional view of one embodiment of the tackfilm shown in FIG. 1;

FIG. 3 is a cross sectional view of a first tack film—reinforcementcomposite material including the tack film of FIG. 2.

FIG. 4 is a cross sectional view of a variation of the tackfilm—reinforcement composite material shown in FIG. 3.

FIG. 5 is a cross sectional view of another variation of the tackfilm—reinforcement composite material shown in FIG. 3.

FIG. 6 is a partial cross-sectional side view of a repaired section ofasphaltic pavement including the tack film—reinforcement compositematerial of any of FIGS. 3-5.

FIG. 7 is a cross sectional view of a strand of reinforcing materialused in one embodiment of the tack film—reinforcement compositematerials of FIGS. 3-5.

FIG. 8 is a cross-sectional view of the strand of FIG. 7 afterimpregnation of the strand with resin.

FIG. 9 is a plan view of a reinforcing grid comprising the strands ofFIG. 8.

FIG. 10 is an enlarged detail of an intersection in the grid shown inFIG. 9.

FIG. 11 shows shear performance of the material of FIG. 2

FIG. 12 is a cross-sectional view of another embodiment of areinforcement.

FIG. 13 is a cross-sectional view of a variation of the embodiment ofFIG. 12.

FIG. 14 is a diagram of an apparatus for making the product of FIG. 12.

FIG. 15 is a cross-sectional view of a section of paving repaired withthe reinforcement of FIG. 12 or 13.

DETAILED DESCRIPTION OF THE INVENTION

This description of the exemplary embodiments is intended to be read inconnection with the accompanying drawings, which are to be consideredpart of the entire written description. In the description, relativeterms such as “lower,” “upper,” “horizontal,” “vertical,”, “above,”“below,” “up,” “down,” “top” and “bottom” as well as derivative thereof(e.g., “horizontally,” “downwardly,” “upwardly,” etc.) should beconstrued to refer to the orientation as then described or as shown inthe drawing under discussion. These relative terms are for convenienceof description and do not require that the apparatus be constructed oroperated in a particular orientation. Terms concerning attachments,coupling and the like, such as “connected” and “interconnected,” referto a relationship wherein structures are secured or attached to oneanother either directly or indirectly through intervening structures, aswell as both movable or rigid attachments or relationships, unlessexpressly described otherwise.

Examples below describe a self adhesive tack film for asphaltic paving,processes for making the film, and methods of forming pavement, in whicha second layer of paving is placed on top of a first layer of paving. Asused herein, the following terms are defined:

Ambient: the surrounding environmental conditions, such as pressure,temperature, or relative humidity.

Strand: a twisted or untwisted bundle or assembly of continuousfilaments used as a unit, including slivers, toes, ends, yarn and thelike. Sometimes a single fiber or filament is also called a strand.

Resinous: of or pertaining to a solid or pseudo-solid organic material,usually of a high molecular weight, which exhibits a tendency to flowwhen subjected to stress or temperature. In its thermoplastic form, itusually has a softening or melting range. Most resins are polymers.

The words “pavings,” “roads,” “roadways,” and “surfaces” are used hereinin their broad senses to include airports, sidewalks, driveways, parkinglots and all other such paved surfaces.

FIG. 1 shows an example of a pavement section 150. During themaintenance and repair of pavement 150, an asphaltic binder course 135is overlaid on top of an existing old pavement 130, which can beconcrete, asphalt, or a mixture thereof. The old pavement 130 istypically texturized, or milled down, by an abrasive roll (not shown),which provides a good gripping surface for the binder course 135. Aprefabricated, resinous or resin-impregnated film 100 places on thebinder course 135 and enhances bonding with surfacing course 140. Thisensures interlayer bonding in the multi-layered paving structure, whichis desirable to decrease the stress distribution that is applied to thesurface course, for example, by motor traffic.

The tack film 100 has first and second major surfaces. The material ofthe tack film 100 at the first and major surfaces thereof is a materialthat is a non-asphaltic resin, or has a composition including about 50%or more of a resin and about 50% or less asphaltic material. Preferably,the material at the surface of the tack film is not more than 25%asphaltic material, and more preferably, the material at the surface ofthe tack film is not more than 20% asphaltic material. In someembodiments, the tack film 100 includes a carrier substrate with aresinous, non-asphaltic material coated on the first and second majorsurfaces thereof, or a material comprising about 50% or more of aresinous, non-asphaltic material and about 50% or less of an asphalticmaterial coated on the first and second major surfaces thereof. In otherembodiments, the entire tack film 100 consists essentially of, orconsists of, a resinous, non asphaltic material; or the entire tack film100 consists essentially of, or consists of a material comprising amajority or plurality portion of a resinous, non-asphaltic material anda non-zero minority portion of an asphaltic material.

In some embodiments, the tack film 100 is suitable for use as asubstitute for the asphalt emulsion that is used as a bonding agentbetween pavement layers 135 and 140. The tack film 100 enhancesinterlayer bonding in the asphaltic road construction.

Because the tack film 100 is a pre-fabricated product, it allows theinstaller to control the application rate and thickness of the tacklayer. The spraying and curing operations (that are performed in situ ifan asphalt emulsion were used) can be eliminated when the tack film 100is used. The tack film 100 expedites road construction through theelimination of these steps on the job site. The tack film 100 canprovide a thickness and shear and fatigue performance that is equivalentto, or better than, that obtained with an asphalt emulsion.

FIG. 2 shows a first example of a tack film, which may be a compositefilm 100. In some embodiments, as shown in FIGS. 1 and 2, a thin polymerfilm 110 is laid over the base layer 135, and functions as a carrier toevenly distribute resin (or a material comprising about 50% or more ofpolymer resin and a about 50% or less of asphaltic material) 120 of thecomposite tack film 100. The resin 120 (or composition of resin andasphaltic material) thoroughly covers both sides of the carrier film 110through a coating process to form a tack composite film 100. Thenon-tacky smooth surfaced nature of the coating provides convenience inhandling at the construction site.

An exemplary process for making a composite tack film 100 is as follows.A first step includes laying a thin resinous or resin-impregnatedpolymer film as carrier film 110. The thin film 110 is then coated witha polymer resin 120 (or composition of resin and asphaltic material),for example, by dipping the film in the resin or composition of resinand asphaltic material. The coated film 100 is then dried. An adhesive122 (such as a pressure sensitive adhesive) may be applied to thebacking side (bottom side after installation) of the coated film. Thenthe adhesive 122 is dried. The adhesive 122 keeps the film in placewhile the overlying surfacing course 140 is applied.

The polymeric resin (or composition of resin and asphaltic material) 120may have a coefficient of thermal expansion (CTE) similar to that ofasphalt 140. Preferably, the polymeric resin (or composition of resinand asphaltic material) has superior stability to that of asphalt 140and 135, with higher stiffness in a broad temperature range. Thecomposite tack film 100 is more visco-elastic than an asphalt basedfilm. When dried, the composite film 100 has a smooth, non-tackysurface. In service, when the hot mix asphalt mixture of surface course140 is applied on the tack composite film 100, the polymeric resin (orcoating composition of resin and asphaltic material) 120 is activated toprovide bonding force, and the attachment between pavement layers 135,140 is enhanced by means of the tack composite film 100.

When an asphaltic spray emulsion was used in road construction, theinstaller had to try to make the asphalt emulsion coating appropriatelythin and uniform for optimal performance. Use of a tack film 100 asdescribed herein provides a predetermined thickness. The uniformity ofthe thickness of coating 120 can be controlled. The thickness of coating120 can be optimized to a thickness equivalent to the optimalapplication rate of an asphaltic emulsion tack coating.

The tack film 100 eliminates steps for in situ spraying and curing ofthe asphalt emulsion. Both time and labor costs for pavementconstruction projects can be reduced. Further, because the in situcuring step is eliminated, the time needed to complete a given area ofpavement is more predictable than when sprayed emulsion is used. Byeliminating installation time unpredictability, it may be possible toeliminate slack time from the installation schedule, increasingefficiency, and further reducing project duration. Additionally, becausethe thickness of the film can be optimized and controlled, wastage ofthe tack film can be reduced. The ability to use a pre-fabricated,mass-produced composite tack film opens the door for possible reductionin material costs.

In some embodiments, the addition of an adhesive 122 on the back of thetack film 100 makes the field installation more secure. Preferably, apressure-sensitive adhesive 122 is used, for easy installation.

In some embodiments, the carrier film 110 may comprise a polyethylenefilm. The carrier may have a thickness from about 0.5 mil to about 10mil, and more preferably, carriers from about 0.5 mil to about 2 mil canbe used. For example, the film 110 may be a low density polyethylenefilm of about 0.5 mil (0.01 mm), although other materials andthicknesses, such as a polyethylene-polypropylene copolymer film about2-mil (0.05 mm) thick could be used. Polyethylene is an inexpensivematerial. Although polyethylene may shrink at a drying temperature ofsome resin coating materials, preferred resins protect the film 110, sothat the film keeps its shape during the drying process. Other polymerfilms that are compatible with asphalt may be used for the carrier layer110 (e.g., PVC, nylon (polyamide), acrylics, HDPE, and certainpolypropylenes, which give the desired rigidity, compatibility, andcorrosion resistance.). In other embodiments, the carrier layer maycomprise a multi-layer sheet made of two or more of these materials, orone of these materials in combination with a different compatiblematerial.

The film 110 may be perforated. Perforations increase the speed ofimpregnation of the resin 120 into the film 110. A network of resin (orcoating composition of resin and asphaltic material) 120 can be formedon both sides of the film 110. Heat from the hot melt asphalt of thesurface layer 140 transfers through the bottom of the film 110 to thelower (binder) asphaltic concrete layer 135.

In some embodiments, the non-asphaltic, resinous coating (or coatingcomposition of resin and asphaltic material) 120 applied to the film 110makes the tack film 100 more compatible with the surrounding asphalticlayers 135, 140. This is accomplished by carefully tailoring thechemical composition of the coating 120 so that there is plastic flow ofthe resin at paving temperatures, pressures, or both. Preferably, thecomposition of coating 120 has a glass transition temperature of greaterthan 68-77° F. (20-25° C.), and preferably undergoes plastic flow attemperatures above about 120-140° F. (50-60° C.). Once the temperaturesof asphaltic paving are reached, i.e., about 265-320° F. (130-160° C.),flow of the coating 120 is possible under even very low pressures. Infact, paving pressure by construction compaction and the weight of thesurface course 140 may effect on some flow for at least localizedconformation to the surfaces which are in very close proximity. Typicaltemperatures of surface course 140 start out at about 250-320° F.(121-160° C.) during installation, and result in temperatures of about140-150° F. (60-66° C.) at the inter-layer tack film 100. This is enoughto heat the tack film 100 and the coating 120 on the film 110. This heatcauses the coating 120 to flow and the film 110 to relax and be “ironedout”, to promote a better mechanical bonding by tack film 100 to thebinder course 135 and the surface course 140 of pavement 150.

The chemical nature of the coating 120 can also allow some degree ofphysical and/or chemical bonding due to Van der Waals attraction to anyexposed aggregate, asphalt or the like. Both the physical and chemicalprocesses improve shear adhesion between the surface course and thebinder course, improving the shear strength. In general, the thicker thecoating 120, the better the shear performance, up to a maximum valuethat is specific to each coating material.

In another preferred embodiment, a method of reducing bending moment inasphaltic paving courses is provided. The method includes applying anasphaltic binder course 135 preferably having a thickness of about 0.75inches (19 mm) or more to an existing road surface 130, followed byapplying a composite tack film 100 to the asphaltic binder course 135.The film 100 may comprise a carrier layer 110 of polyethylene, ethylenevinyl acetate (EVA) or other suitable polymer. A resinous non-asphalticcoating (or coating composition of resin and asphaltic material) or film120 is disposed over the carrier film 110 in composite layer 100. Thecoating or film (hereafter collectively referred to as “surface layer”)120 is activated (thermoplastic) at a paving temperature, pressure, orboth, to form a bond compatible with asphaltic paving 135, 140. Thesurface layer 120 may comprise a thermoplastic resin which plasticallyflows at a paving temperature, pressure, or both, but which is not tackyat an ambient temperature and pressure. The method further includesapplying an asphaltic surface course 140 having a thickness of about 1.5inches (40 mm) or more over the composite tack film 100, asphalticbinder course 135 and the existing load surface 130. The pressure andheat of the surface course 140 causes the thermoplastic resin 120 toplastically flow to improve the interlaminar bond between the asphalticbinder course 135 and the asphaltic surface course 140. The interlaminarbond can be an adhesive, melt or chemical (and/or Van der Waals) bond,or a combination thereof.

In some embodiments, the surface layer 120 is an acrylic coating. Insome embodiments, the surface layer 120 may comprise a polyvinylchloride (PVC) latex emulsion coating comprising about 1-8 wt. % waxrelease agent, and about 0-10 wt. % additives selected from the groupconsisting of: soluble polymer, ammonia, thickener, carbon black,defoamer, and plasticizer. One preferred PVC latex emulsion is Vycar®460x63 latex (vinyl emulsion) available from Noveon, Inc., Cleveland,Ohio, which provides a great degree of plastic flow at pavingtemperatures greater than about 120-140° F. (49-60° C.) at the coatingsurface. There may also be an innate level of chemical adhesion of thePVC latex polymer to asphalt.

In some embodiments, the coating comprises 40-60% Vycar® 460x63 latex,and in some embodiments, the coating comprises at least about 40% Vycar®460x63 latex and up to about 20% asphaltic material. In someembodiments, the coating comprises 45-50% Vycar® 460x63 latex, and insome embodiments, the coating comprises at least about 45% Vycar® 460x63latex and up to about 5% asphaltic material.

By itself, Vycar® 460x63 in known to be fairly rigid, particularly incold weather. This could cause installation problems when the coatedfilm 100 is applied around curves in the road. Vycar® 460x63 is alsoless resistant to liquid water than other resinous candidates. Since itssolids level is rather low, it may be harder to get the desired pick-uplevel, and once absorbed, it may be more difficult to dry the fabricadequately.

Accordingly, in some embodiments, the coating 120 containing Vycar®460x63 is formulated in such a way as to make the coating softer, andincrease its solids level.

The polymer in the coating 120 can also be made from softer monomers.The water repellency issue may be cured by incorporating a wax additivesuch as Hydrocer 145 at a level of about 3-5 wt. % of the dry coating.This wax release agent also has a tendency of softening the coatingslightly. The solids level of the coating may be improved to about 50-60wt. %, ideally about 55 wt. % or more. In addition to these improvementsto the PVC latex, a soluble polymer such as Carboset 514W, in amounts ofabout 5-9 wt. % of the dry coating, can be introduced to give more opentime and re-wetability to the coating on the pad rolls. Other watersoluble polymers, such as Michemprime polymer, may be used.

In order to activate the soluble polymer, ammonia can be added to a pHof about 8 or 9. The ammonia can also be used to activate any alkalisoluble thickeners used in the composition. Such thickeners can includethose commonly available, and are preferably used if the pick-up targetcan not be obtained. ASE-60 or 6038A from Rohm and Haas, Philadelphia,Pa., would be useful for this application.

Colorants such as carbon black in the amount of about 1 wt. %, anddefoamers to a level of about 0.05 wt. %, such as NXZ or DEFO, areuseful for this application.

Finally, a plasticizer can be used to obtain the desired softness in thecoating. ADMEX 314 is desirable since it is a non-volatile polymericplasticizer and will not cause environmental or health hazards, andlevels of about 2-5 wt. % make a significant difference in the softnessof the coating.

Many alternative types of resins may be used for surface layers 120,provided they plastically flow at paving temperature, pressure, or both.Primary examples are PVC, nylon, acrylic, HDPE, and certainpolyethylenes and polypropylenes, and ethylene vinyl acetate (EVA) whichgive the desired rigidity, compatibility, and corrosion resistance. Theymay be applied using hot-melt, emulsion, solvent, therma-cure orradiation-cure systems. In some embodiments, tack film 100 includes amultilayer film. For example, the carrier layer 110 may be a multilayerfilm with a surface layer coating 120 applied thereon. In otherembodiments, the entire tack film 100 is a co-extrusion, and the surfacelayers 120 are resin films that are co-extruded with the carrier layer110. The material of surface layer 120 may be the same as the materialof the carrier layer 110, may include the same majority constituent ascarrier layer 110, or may have a different majority constituent thancarrier layer 110.

When any of these alternative resin materials are used for surface layer120, an anti-blocking agent (e.g., wax, synthetic polymer, light dustingof talcum powder) may be included in surface layers 120 to prevent thetack film 100 from sticking to itself when stored in a spiral roll formand pulling away from the grid 10 during subsequent unrolling. A slipagent may also be included in the surface layers 120 on one or bothsides of the carrier layer 110.

The above compositions are significantly compatible with asphalticsurface 140 and binder 135 courses. They permit strong bonding to theembedded tack film 100 in asphaltic concrete. The sturdy adhesionbetween layers of paving effectively decreases stress distribution tothe surface layer by traffic. Such a solution can prevent slippage,cracking and de-lamination, known as premature stresses, caused or aidedby lack of interface bonding.

A coefficient of thermal expansion of surface layer 120 approximatesthat of an asphaltic mixture. The surface layer 120 possibly avoidsundesirable disengagement at the interface of the film 100 due todiscrete thermal behavior in composite asphaltic concrete. The enhancedinterfacial condition bestows an extended service life on the overlaidsurface asphaltic layer 140 against prominent road stresses.

An example is described above in which the carrier film 110 comprises afirst material (e.g., a polymer, such as polyethylene), and the film 110is coated with a second material 120 (e.g, Vycar® 460x63 with additives,as described above). However, other embodiments are contemplated, inwhich the film 110 consists essentially of (or consists of) thenon-asphaltic, resinous material that is described above for use as thecoating material 120 (e.g, Vycar® 460x63 with additives). In suchembodiments, the separate layer of coating material 120 may be omitted.Thus, the tack film layer may be a composite film 100 or a homogeneousresinous film. The choice of whether to use a composite or homogeneousfilm, and the choice of material for the carrier film 110, may depend onmaterial cost, ease of manufacture, and commercial availability of eachmaterial, as can readily be evaluated by one of ordinary skill at anygiven time.

When impregnated and coated with a resinous coating or coextruded with aresinous film 120, the film 100 is, preferably, semi-rigid, and can berolled-up on a core for easy transport as a prefabricated, continuouscomponent to the place of installation, where it may be readily rolledout continuously for rapid, economical, and simple incorporation intothe roadway. For example, film 100 can be placed on rolls 15 feet (4.5meters) wide containing a single piece 100 meters long or longer.Alternatively, the binder course 135 may be covered by several narrowerstrips of film 100, typically, each about five feet (1.5 meters) wide.It is, therefore, practical to use this film 100 on all or substantiallyall of the surface of binder course 135, which is cost effective becauseof reduced labor.

At the paving site, the film 100 is unrolled with the adhesive 122facing downwards and laid on the underlying paving 135 which ispreferably about 40-140° F. (4.4-60° C.) upon application of the film100.

The tack film 100 is rolled out and adhered to the underlayment layer,or asphaltic binder course 135, which is preferably about 0.75 inches(19 mm) or more in thickness. In some embodiments, before any overlay orasphaltic surface course 140 is placed on top of the film 100, the film100 can be made sufficiently stable, such as by an adhesive 122 (e.g.,pressure-sensitive adhesive) applied during manufacture of film 100, sothat the film 100 resists the action of workmen walking on it,construction vehicles traveling over it, and, particularly, the movementof the paving machine over it.

The film 100, though semi-rigid, tends to lie flat. It has little or notendency to roll back up after having been unrolled. This is believed tobe due to the proper selection of binder and/or surface layer resin.

In some embodiments, as shown in FIGS. 1-2, the resurfaced pavementincludes the pavement 130 to be resurfaced, the base layer 135, tackcomposite film 100, and surface layer 140, without a separatereinforcing layer.

In other embodiments, the tack film 100 is applied over the binder layer135, a separate reinforcing layer is applied over the tack film 100, andthe surface layer 140 is applied over the reinforcing layer. Forexample, the reinforcing layer may be a commercially available GlasGrid®product (e.g., 8550, 8501, 8502, 8511 or 8512 grid) from Saint GobainTechnical Fabrics.

In other embodiments, shown in FIGS. 3-6, the tack film 100 is includedin a unitary composite reinforcing interlayer 200, 300, or 400. Theunitary composite material 200, 300 or 400 includes a tack film layer100 and a reinforcing layer 10.

In some embodiments, the composite reinforcing interlayer is a composite200 (FIG. 3) comprising a composite or resinous tack film layer 100above a reinforcing layer 10. The tack film layer 100 is bonded to thereinforcing layer 10 with adhesive 12, which may be a hot melt adhesive.The hot melt adhesive may be pressure sensitive or permanent. The bottomsurface of the reinforcing material 10 (facing away from the tack filmlayer 100) has an adhesive 11, such as a pressure sensitive adhesive,which keeps the composite material 200 in place while the surfacingcourse is being applied. In the configuration of FIG. 3, the hot meltadhesive layer 12 bonds the tack film layer 100 to the underlyingreinforcing layer 10, so the tack film layer 100 does not require itsown adhesive layer 122. Also, the surface course 140 contacts the top ofthe film layer 100, and does not need an adhesive layer 122 on the uppersurface of the film 100. Adhesive layer 122 may be omitted from the tackfilm 100 to be used in the composite material 200 of FIG. 3.

In some embodiments, the composite reinforcing interlayer is a composite300 (FIG. 4) comprising a reinforcing layer 10 above a composite orresinous tack film layer 100. The tack film layer 100 is bonded to thereinforcing layer 10 with adhesive 12, which may be a hot melt adhesive.To ensure that the composite material 300 remains in place while thesurface course 140 is being applied, the tack film 100 in compositematerial 300 includes the adhesive 122 on its bottom surface (whichcontacts the leveling course 135), as shown in FIG. 2.

In some embodiments, the composite reinforcing interlayer is a composite400 (FIG. 5) comprising a reinforcing layer 10 sandwiched between a pairof composite or resinous tack film layers 100. It will be understoodthat in each of the descriptions below, the tack film 100 may be eithera composite having a carrier layer 110 and a surface layer 120, or ahomogenous film of a material suitable for use in the coating of thesurface layer 120, wherein the homogenous film does not have a distinctcarrier layer 110 therein. In composite 400, the tack film layers 100are bonded to the reinforcing layer 10 with adhesive 12, which may be ahot melt adhesive. To ensure that the composite material 400 remains inplace while the surface course 140 is being applied, the bottom tackfilm 100 (which contacts the leveling course 135) in composite material400 includes the adhesive 122 on its bottom surface, as shown in FIG. 2.The top tack film layer 100 (which contacts the surface course 140) doesnot require the adhesive 122 on surface thereof. The adhesive 122 may beomitted from the top tack film layer 100.

The reinforcing layer 10 may be any of a variety of reinforcingmaterials. In some embodiments, an open grid (shown in FIGS. 9 and 10)comprising at least two sets of substantially parallel strands 21 (shownin cross section in FIGS. 7 and 8) is provided as the reinforcing layer10. Each set of strands 21 includes openings 19 (FIG. 9) betweenadjacent strands 21, and the sets are oriented at a substantial angle toone another (e.g., optionally approximately 90 degrees). In someembodiments, the reinforcing layer may be a GlasGrid® product (e.g.,8550, 8501, 8502, 8511 or 8512 grid) from Saint Gobain TechnicalFabrics.

In some embodiments, the grid 10 preferably comprises a weft-insertedwarp knit in which the strands 21 are oriented at about a 90° angle toone another, as shown in FIG. 9. The openings preferably have adimension of about 0.5 inch×0.5 inch (12 mm×12 mm) or larger, althoughthe openings may be as large as approximately 1 inch×1 inch. Althoughthe openings 19 can be square, the dimensions “a” and “b” may bedissimilar, such as in the case of a rectangle.

In some embodiments, a non-asphaltic coating 22 is disposed over thegrid 10 without closing the openings between the strands 21, as bestseen in FIG. 8. The coating 22 is activated at a paving temperature,pressure, or both, to form a bond compatible with asphaltic paving. Thecoating 22 is not tacky at ambient temperature and pressure so that itcan be handled easily at a job site. In some embodiments, the coating 22on the strands 21 is the same material as the coating 120 that isapplied to the polymeric film 110 in the composite tack film 100.

The large grid openings 19 shown in FIG. 9 permit the asphalt mixture135 and/or 140 to encapsulate each strand 21 of yarn 20 or rovingcompletely, and permit complete and substantial contact between the tacklayer 100 and both the binder and surface courses 135 and 140. The tacklayer 100 substantially bonds layers 135 and 140 through the openings 19of the grid 10 to permit substantial transfer of stresses from thepavement 135, 140 to the glass or similar fibers of reinforcing layer10. The resulting composite grid material has a high modulus and a highstrength to cost ratio, its coefficient of expansion approximates thatof road construction materials, and it resists corrosion by materialsused in road construction and found in the road environment, such asroad salt.

The grid 10 may be formed of strands or yarns 21 of continuous filamentglass fibers, though other high modulus fibers, such as polyamide fibersof poly(p-phenylene terephthalamide), known as Kevlar®, may be used. ECRor E glass rovings of 2000 tex and preferred, though one could useweights ranging from about 300 to about 5000 tex. The preferredfiberglass yarns have a strand strength of about 560 lb/in. (100 kN/m)or more when measured in accordance with ASTM D6637, with an elongationat break of 5% or less. These strands preferably have a mass/unit areaof less than about 22 oz/yd² (740 g/m²), and more preferably about 11oz/yd² (370 g/m²).

These strands, which are preferably low twist (i.e., about one turn perinch or less), are formed into grids with rectangular or square openings19, preferably ranging in size from ¾ inch to 1 inch on a side(dimensions “a”, “b”, or both in FIG. 9), though grid openings 19ranging from ⅛ inch to 6 inches on a side (“a”, “b”, or both) may beused.

The grids 10 are preferably stitched with thread 25, shown in FIG. 10,or otherwise fixedly connected at the intersections of the crosswise andlengthwise strands. This connection holds the grid 10 in its gridpattern, prevents the strands 21 from spreading out unduly before andduring impregnation by the non-asphaltic coating 22, and preserves theopenings 19, which permit the overlayment to bind to the underlyinglayer and thereby increase the strength of the final composite roadwayrepair 100.

The fixed connections at the intersections of the grid 10 alsocontribute to the strength of the grid 10 because they permit forcesparallel to one set of strands 21 to be transferred in part to the otherset of parallel strands 21. At the same time, this open gridconstruction makes possible the use of less glass per square yard andis, therefore, a more economical product than a closed woven fabric, forexample. We prefer to use a grid 10 of about 8 ounces per square yard,though 4 to 24 ounces per square yard may be used.

While we prefer stitching grid intersections together on warp-knit,weft-insertion knitting equipment using 70 to 150 denier polyesterthread 25, or equivalent, other methods of forming grids withfixedly-connected intersections may be utilized. For example, anon-woven grid made with thermosetting or thermoplastic adhesive mayprovide suitable strength.

Once the grid 10 is formed, and before it is joined to the tack film100, a resin, preferably a thermoplastic resin 22, is applied. That isto say, the grid 10 is “pre-impregnated” with resin 22.

The viscosity of the resinous coating 22 is selected so that itpenetrates into the strands 21 of the grid 10. While the resinouscoating 22 may not surround every filament 20 in a glass fiber strand21, the resinous coating 22 is generally uniformly spread across theinterior of the strand 21, as shown in FIG. 8. This impregnation impartsa preferable semi-rigid nature to the strand 21, and cushions andprotects the strands 21 and glass filaments 20 from corrosion by water,salt, oil and other elements in the roadway environment. Theimpregnation also reduces abrasion between glass strands 21 or filaments20 and the cutting of one glass strand 21 or filament 20 by another. Theimpregnation also reduces the tendency of the glass fibers to cut eachother after the grid has been laid down, but before the overlayment 140has been applied.

The grid should preferably have a minimum strength of about 25 kN permeter (kN/m) in the direction of each set of parallel strands, morepreferably about 50 kN/m, and most preferably, about 100 kN/m or more,with preferably less than about 10%, and more preferably less than 5%elongation at break.

While drying or curing the preferred resinous coating 22 on the grid 10,the strands 21 may be somewhat flattened, but the openings 19 aremaintained. For example, in a preferred embodiment using 2000 texrovings, a rectangular grid 10 may be formed with openings 19 of about ¾inch by one inch (a=b=0.75 in.), and the rovings flattened to about 1/16inch (1.6 mm) to ⅛ inch (3.2 mm) across. The thickness of the rovingsafter coating and drying can be about 1/32 inch (0.8 mm) or less. Apreferred grid of glass fiber strands is uncoated GlasGrid® product(e.g., 8550, 8501, 8502, 8511 or 8512 grid) available from Saint-GobainTechnical Fabrics.

Many resins can be used for impregnating the grid 10 provided theyplastically flow at paving temperature, pressure, or both. Primaryexamples are PVC, nylon, acrylic, HDPE, and certain polyethylenes andpolypropylenes, which give the desired rigidity, compatibility, andcorrosion resistance. They may be applied using hot-melt, emulsion,solvent, therma-cure or radiation-cure systems, for example, a coatingcontaining a PVC emulsion such as Vycar® 460x63. The PVC emulsion couldalso include about 1-8 wt. % wax release agent, and about 0-10 wt. % ofone or more other additives selected from the group consisting ofsoluble polymer, ammonia, thickener, carbon black, defoamer, andplasticizer. Any material suitable for use as the coating 120 (such asany of the materials described above) of composite polymer film 100 maybe used as the coating 22 for the grid 10. In some embodiments, coatings120 and 22 are the same material. In other embodiments, coatings 120 and22 are different materials, wherein each coating 120, 22 is compatiblewith asphalt and activatable by heat and/or pressure.

The coatings 120 and 22 are activatable by pressure, heat, or othermeans. A pressure activatable resin forms a bond when a surface coatedwith it is brought into contact with a second untreated surface, andpressure is applied. A heat activatable resin forms a bond when asurface coated with it is brought into contact with an untreated surfaceand heat is applied. As compared with other adhesives which are tacky atambient temperatures (e.g., about 72° F.) and pressures (e.g., about 1atmosphere), the coatings 120 and 22 are preferably not tacky at ambienttemperature or pressure, and only become so at approximately pavingpressure or temperature.

In most uses, the coatings 120 and 22 do not plastically flow or adhereuntil a coating temperature of about 120-140° F. (49-60° C.) is reached,or a paving course of about 1-1.5 inches (25-38 mm) or more in thicknessis applied, or both. The melting point of the E-glass fiber is about1800-1832° F. (about 1000° C.), which ensures stability when subjectedto the excessive heat of a paving operation.

It is desirable that the shear strength between the surface course 140and binder course 135 be as high as possible, and that the shearstrength be substantial over the extremely broad range of temperaturesto which the grid 10 will be subjected. The tack film-grid composite200, 300 or 400 may be installed on paving underlayments at ambienttemperatures as low as about 40° F., and asphaltic concretes may beapplied at temperatures of about 250-320° F. (121-160° C.), generallyabout 300° F. (149° C.), raising the coating 22 temperature to about150° F. (66° C.). We therefore prefer that coatings 120 and 22 have amelting point or glass transition temperature, Tg, of about 66-77° F.(20-25° C.) or higher, and that they preferably plastically flow aboveabout 120-140° F. (50-60° C.) under typical pressures exerted by paving.

Once temperatures of about 265-300° F. (130-150° C.) are achieved, flowis possible even at very low pressures, such as when very thin asphalticlayers are applied. This would enable plastic flow of the coatings 120and 22 to improve shear strength between the surface and binder courses140 and 135 in and around the grid 10.

The viscosity of the coatings 120 and 22 should be sufficiently fluid toflow onto the grid, but preferably is sufficiently viscous that it doesnot flow out of or through the grid during application or storage, butrather stays on the grid.

Example 1

The coating 22 described in Table 1, below, was prepared and applied toan uncoated GlasGrid® product (8501 or 8511 grid) from Saint GobainTechnical Fabrics:

The preferred resin systems useful for the coatings 120 and 22 includethose that are liquid, or can be liquified, for impregnating some or allof the spaces between the filaments 20. The resin system should beactivated at paving temperature, pressure, or both, to form a bondcompatible with asphaltic paving. Such systems may include thermosettingresins, such as B-stage epoxy, silicone, or phenolic; or thermoplastics,such as nylon, polyethylene, polypropylene, polyurethane or polyvinylchloride. Plastisols including resin and solvent mixtures or neat resin,with or without additives, are useful alternatives. Preferredingredients and ranges for a desirable polyvinyl-chloride latex emulsionsystem are provided in Table 1, below:

TABLE 1 Preferred PVC Coating Ranges Broad Narrow Commercial range dryrange dry Generic Description Name wt. % wt. % base PVC-acrylic latexVycar 460x63 40-60 45-50 internally plasticized Vycar 578  0-20  7-14PVC latex styrene-acrylic latex Rhoplex  5-25 15-20 AC-1035ethylene-acrylic acid Michemprime  5-25 12-18 latex 4983-40R organicoils/silica DeeFo 97-3 0-1 0.1-0.3 defoamer carbon black dispersionHelzarin black 0-5 0.5-2   EBS anti-blocking wax Hydrocer 145 0-5 1-3dispersion acrylic solution polymer Carboset 514  0-10 1.5-3.5 non-ionicsurfactant Sryfynol 104 0-1 0.05-0.15 PA non-ionic surfactant Sryfynol104 0-1 0.05-0.15 PG 50 fluorosurfactant Zonyl FSO 0-1 0.05-0.15saturated aqueous 28% ammonia 0-1 WET % 0-0.1 WET % ammonia poly acrylicacid ASE-6038A 0-5 0.25-1/0  thickenerDeeFo 97-3 can be replaced by Foam Blast or Dow Corning 1430 siliconedefoamersHelzarin black can be replaced by Octojet black 104ASE-6038A can be replaced by ASE-60

When impregnated and coated with a resinous, non-asphaltic coating 22(FIG. 8), the tack film-grid composite 200, 300 or 400 (FIGS. 3-5) ispreferably semi-rigid, and can be rolled-up on a core for easy transportas a prefabricated, continuous component to the place of installation,where it may be readily rolled out continuously for rapid, economical,and simple incorporation into the roadway. For example, it can be placedon rolls 5 feet (1.5 meters) wide containing a single piece 100 yards orlonger. The installation procedure for the tack film-grid composite 200,300 or 400 may be the same as described above with reference to theseparate tack film 100. It is, therefore, practical to use this tackfilm-grid composite 200, 300 or 400 on all or substantially all ofpavement surface. It can also be used to reinforce localized cracks 231(FIG. 6), such as expansion joints.

The grids 10, though semi-rigid, tend to lie flat. They have little orno tendency to roll back up after having been unrolled. This is believedto be due to the proper selection of binder and/or coating resin and theuse of multifilament reinforcing strands, preferably of glass, in thegrid 10.

The large grid openings 19 shown in FIG. 9 permit the asphalt mixture toencapsulate each strand 20 of yarn 21 or roving completely, and permitcomplete and substantial contact between the composite 200, 300, 400 andthe binder and surface courses 135 and 140. The surface course 140preferably is disposed in a thickness of about 1.5 inches (40 mm) ormore. The resulting composite 200, 300, 400 has a high modulus and ahigh strength to cost ratio, its coefficient of expansion approximatesthat of road construction materials, and it resists corrosion bymaterials used in road construction and found in the road environment,such as road salt.

From the foregoing, it can be realized that the self adhesive tack filmmay be used in a reinforcement for asphaltic paving, either alone, or incombination with an open grid and a resinous, coating which is activatedat paving temperature, pressure, or both, to form a bond compatible withasphaltic paving.

Example 2

Polymer Resin Coated Film Preparation

A thin polyethylene (PE) and polypropylene (PP) blended film of 12.7micrometers in thickness was prepared. The film was perforated withopenings of 0.5 millimeter diameter every 25.4 millimeters at intervalto ease heat transfer from the hot mix asphalt mixtures of the surfacelayer application to the lower asphalt layer, and to let the film adhereto the asphalt pavement layers. The film was dipped into a bulkpolymerized (vinyl chloride) PVC acrylic copolymer in emulsion at 21° C.and the coated film was dried for 2 minutes in the convection oven at100° C. until a residual rate of 123 gram per meter2 of coating on thefilm was achieved.

The film is preferably a synthetic material to carry the polymeric resinwith strong adhesion to the asphaltic system. Illustrative of, but notlimiting, the thin films which can be used are the following:

Polyethylene Polypropylene

Polyethylene and polypropylene copolymer

Polyester

Polyvinyl chloride

Fibreglass mat

Thermoplastic polyolefinEthylene vinyl acetate

Some of the preferred polymers which may be used in preparing thenon-asphaltic resins include acrylic copolymer, i.e., acrylic copolymerand polyvinylchloride acrylic copolymer.

Table 2 provides mechanical testing data for various films of differentsubstrate materials, on which a PVC acrylic copolymer coating wasapplied at a rate of 123 gram per meter2. The tested substrate materialsincluded a blended film of PE and PP (Sample 1); a film of polyester(Sample 2); a film of thermoplastic polyolefm (Sample 3) and a mat offiberglass (Sample 4).

TABLE 2 Mechanical Testing Data Substrate Materials (thickness inTensile at Break* Shear at Break** Samples micrometer) (N/mm² (N/mm² 1PE (80%)/PP (20%) 1.91 1.24 (12.7) 2 Polyester 9.44 1.03 (12.2) 3Polyolefin 5.14 1.54 (25.4) 4 Fibreglass mat 13.83 0.92 (254) *Tensiletesting followed ASTM D638-02a protocol at 60% humidity at 21° C.**Mechanical bonding of films in paving system was determined bymeasuring shear strength on bituminous cylindrical specimens four inches(100 millimeters) in diameter, which were prepared by using Marshallapparatus according to ASTM D6926-04. Each film was placed in a specimenincluding two asphaltic layers and sheared at a constant displacementrate of 1 millimeter per minute.

A pressure sensitive adhesive 11 may be applied to the bottom of thegrid 10 during fabrication of the grid 10 or composite product 200, tofacilitate installation, where the grid 10 is the bottom layer of thecomposite 200 upon installation. The adhesive 11 may be of a differenttype from the hot melt adhesive 12 used to attach the pre-coated film100 onto the grid 10. If present, the pressure sensitive adhesive 11 isactivated by applying pressure to the surface of the polymer resincoated film 100 of composite 200. If a pressure sensitive adhesive 11 isused, substantial force may be required to unroll the film; a tractor orother mechanical means may be used. The adhesive 11 is preferably asynthetic material and may be applied to the pre-coated film in anysuitable manner, such as by use of a latex system, a solvent system, ora hot melt system. In a preferred latex system, the adhesive 11 isdispersed in water, printed onto the film using a gravure print roll,and dried. In a solvent system, the adhesive is dissolved in anappropriate solvent, printed onto the film, and then the solvent isevaporated. In the hot melt system, the adhesive may be melted in areservoir, applied to a roll, and metered on the roll with a closelycontrolled knife edge to create a uniform film of liquid adhesive on theroll. The grid 10 is then brought into contact with the roll and theadhesive transferred to the bottom of grid 10. These application methodsare only exemplary, and other methods may readily be selected by thoseof ordinary skill in the art for applying the adhesive using a latex,solvent, or hot melt system.

Example 3

FIG. 11 is a plot of data from a series of trials conducted oncompositions for use in the coating 120 and/or coating 22. The data wereused to determine what percentage of asphaltic emulsion could be blendedwith the non-asphaltic resinous material used in the coating 120 withoutsubstantially degrading the shear performance relative to the shearperformance of a non-resinous coating.

Asphalt emulsion was blended with the polymer resin described in Table1, with the relative amounts based upon percentage of dry weight. Theblended resin was prepared using 6 different resin/asphalt ratios;polymer vs. asphalt (100% resin, 75:25, 50:50, 25:75, 10:90, 0:100).

A non-coated e-glass grid fabric, called “greige”, was manually dippedinto the resin or resin/asphalt mixture and thoroughly impregnated anddried out. The manually coated fabric was placed in between a pair ofasphalt pucks (four-inch diameter cylindrical shaped samples). Each puckwas constructed with asphalt mixes under 146° C. by 75-blow standardMarshall compactor according to ASTM D6926-04. Shear performance wasconducted by means of direct shear testing method.

As shown in FIG. 11, the shear strength varied from 1 kN for a pureasphaltic coating to 3.68 kN for 100% non-asphaltic resin. From a curvefitting the data points, at about 30% resin, the shear strength is abouttwice that of the asphaltic emulsion alone. At about 50% resin, theshear strength is about 2.4 times that of the asphaltic emulsion. Atabout 75% resin, the shear strength is about 3.5 times that of theasphaltic emulsion. With about 80% resin, the shear strength of about3.5 kN is nearly as high as the shear strength (about 3.7 kN) of the100% polymer resin. Thus, mixtures of about 75% to about 80% resinprovide nearly the full strength of the 100% resin coating, whileproviding greater economy.

Thus, if a blended coating is to be used, the material used for thesurface layer 120 of the tack film 100 preferably includes 50% or moreof the non-asphaltic polymer resin in the blend with the asphalticemulsion.

FIGS. 12-14 show another embodiment. FIG. 12 shows a product 500comprising first and second non-woven polymer substrates 501, a layer ofreinforcing fibers 510 sandwiched between the non-woven polymersubstrates 501, and an adhesive 512 joining the layer of reinforcingfibers to the non-woven substrates. The mesh or scrim 510 is bonded tothe substrates 501 and made into rolls in any of a variety of widthsand/or lengths.

In some embodiments, the substrates 501 may comprise polyester non-wovenfelt webs. The polyester non-woven substrates are each nominally 17.0g/m2 or 0.5 oz/yd² in weight. Thickness of each is 0.14 mm or 0.0056″.These polyester non-wovens are commercially available from Shalag ShamirNon-wovens of Upper Galilee, Israel. In other embodiments, substrates501 may be a polyethylene non-woven felt, although other materials, suchas a polyethylene-polypropylene copolymer could be used. Other polymersthat are compatible with asphalt may be used for the substrates 501(e.g., PVC, nylon (polyamide), acrylics, HDPE, and certainpolypropylenes, which give the desired rigidity, compatibility, andcorrosion resistance.). In other embodiments, the substrates 501 maycomprise a multi-layer sheet made of two or more of these materials, orone of these materials in combination with a different compatiblematerial.

The layer of reinforcing fibers 510 includes fiber glass mesh or scrimincluding at least a first set of yarns oriented substantially in amachine direction. The yarns may comprise ECR or E-glass filaments. Inother embodiments, other high modulus fibers, such as polyamide fibersof poly (p-phenylene terephthalamide), known as “KEVLAR®,” may be used.

The adhesive 512 is capable of being activated at a paving temperature,pressure, or both, to form a bond compatible with asphaltic paving.Preferably, the adhesive 512 comprises 50-99 wt. % PVC latex emulsion.In some embodiments, the adhesive 512 is the PVC latex emulsiondescribed above in Table 1.

Referring now to FIG. 12, in some embodiments, the product includes meshor scrim 510 of reinforcing fiber coated yarns (e.g., fiber glass) andtwo polyester nonwoven substrates 501. The fiber glass mesh or scrim 510is formed by “turbine technology.” Turbine technology involves the useof a rotating turbine head equipped with cross direction yarns andutilizing a machined spiral mechanism to control the cross directionspacing of the yarns. The fiber glass scrim 510 is then impregnated andcoated with a binder. Many resins can be used for the binder, providedthey plastically flow at paving temperature, pressure, or both. In someembodiments, the binder is the PVC latex emulsion described above inTable 1. In other embodiments, the binder may be acrylic, PVC, nylon,HDPE, and certain polyethylenes and polypropylenes, which give thedesired rigidity, compatibility, and corrosion resistance. The bindermay be applied using hot-melt, emulsion, solvent, therma-cure orradiation-cure systems. Immediately after coating the yarns with thebinder, the scrim 510 is laminated to the two polyester substrates 501using adhesive 512.

In some embodiments, the adhesive 512 and the binder are both the samePVC latex emulsion described above in Table 1, and a single applicationstep is used to impregnate the yarns with the binder/adhesive and coatthe yarns with adhesive 512 for the lamination steps. In otherembodiments, the adhesive 512 may be applied separately from the step ofimpregnating the yarns 510 with binder. For example, a separate adhesiveapplying step would be used if the binder and adhesive 512 are differentmaterials from each other.

After the mesh or scrim 510 are coated, the product 500 is then cured(e.g., in the drying section of the machine) and wound into finishedrolls. The result is a tri-laminated product 500 with fiber glass scrim510 sandwiched between a top layer 501 and a bottom layer 501 ofpolyester non-woven substrate.

FIG. 14 shows one example of an apparatus for making the product of FIG.12. The top and bottom substrates 501, which may be a polyesternon-woven material, are fed from rolls 552. The direction of thesubstrates 501 may be controlled by feed rollers 558. The fiber glassscrim 510 is fed by way of another roller 558 and passes through avessel containing the coating 512, which coats the scrim 510. The coatedscrim 510 emerges from the coating vessel and is redirected by one ormore rollers 560, 561. The top non-woven layer 501 and the coated scrim510 then pass under a first laminating roll 554, while tension ismaintained between a second laminating roll 556 and the roller 561, tojoin the scrim to the top non-woven layer 501. The top non-woven layer501, with scrim 510 laminated thereto, is then fed past anotherlaminating roller 556, which joins the bottom non-woven substrate 501 tothe bottom of the scrim 510 to form the product 500. The laminatedproduct 500 then is fed to the drying oven (not shown).

In other embodiments (e.g., FIG. 13), the fiber glass scrim includes afirst set of yarns 510 m extending in the machine direction and a secondset of yarns 510 c oriented substantially in a cross direction. In someembodiments, the scrim 510 c, 510 m includes three yarns per inch (aboutone yarn per centimeter) in both the machine and cross directions. Aproduct having three yarns per inch is suitable for use in pavements inlow traffic areas. A larger count of yarns per inch may be used toprovide greater reinforcement, for areas of moderate traffic.

The product 600 (FIG. 13) may be made using the same machine as product500 (FIG. 12), with a few modifications to the process. The crossdirection yarns 510 c are laid on top of the machine direction fibers510 m, and are substantially perpendicular to the machine direction. Thetop layer 501 t of polyester is fed from the top, but is run with thescrim 510 m, 510 c through the coating pan and coating rolls (notshown). This is done to maintain the yarn spacing in the finishedproduct 600 (with scrim 510 c between the top layer 501 t and the scrim510 m). The bottom layer 501 b of polyester is applied in the samemanner as described above, immediately after the binder/adhesive 512 isapplied to the scrim, just as it leaves the coating rolls.

FIG. 15 shows a pavement configuration 550 using the product 500 (FIG.12) or 600 (FIG. 13). During the maintenance and repair of pavement 550,an asphaltic binder course 235 is overlaid on top of an existing oldpavement 230, which has a crack 231. The old pavement 230 is typicallytexturized, or milled down, by an abrasive roll (not shown), whichprovides a good gripping surface for the binder course 235.(Alternatively, the products 500 and 600 may be laid over newasphalt/portland cement concrete pavement surface).

A bitumen tack coat is applied, for example as a hot spray or emulsion.The application rate may be from about 0.1 gallons/yard² to about 0.3gallons/yard². After the bitumen is sprayed, the product 500 or 600 isrolled into the bitumen by either mechanical or manual means. Thebitumen forms a bond between the product 500, 600 and the binder course235, and is also absorbed into the product 500 or 600 to form awaterproofing membrane. Then the asphalt concrete overlay 240 is appliedin one of a variety of thicknesses.

Although the invention has been described in terms of exemplaryembodiments, it is not limited thereto. Rather, the invention should beconstrued broadly, to include other variants and embodiments, which maybe made by those skilled in the art without departing from the scope andrange of equivalents of the invention.

What is claimed is:
 1. A paving composite comprising: a polymericcarrier substrate having first and second major surfaces; and a surfacelayer material disposed on the first and second major surfaces of thepolymeric carrier substrate, the surface layer material comprising aresinous non-asphaltic material or a material including about 50% ormore resinous nonasphaltic component and about 50% or less of asphalticcomponent; wherein the surface layer material of the paving composite isconfigured to bond an underlying layer of paving material to anoverlying layer of paving material, and wherein the surface layermaterial of the paving composite is not tacky at a temperature of about20° C. and a pressure of about one atmosphere.
 2. The paving compositeof claim 1, wherein the polymeric carrier substrate comprises athickness of up to about 10 mil.
 3. The paving composite of claim 1,wherein at least one of the overlying layer of paving material and theunderlying layer of paving material comprises asphalt.
 4. The pavingcomposite of claim 1, wherein the surface layer material of the pavingcomposite is configured to bond the underlying layer of paving materialto the overlying layer of paving material at a surface layer materialtemperature of about 120° C. or more and a pressure that is applied tothe paving composite by the overlying layer of the paving materialhaving a thickness of about 3.8 cm (1.5 inch) or more laid.
 5. Thepaving composite of claim 1, wherein the paving composite is configuredfor storage in a roll.
 6. The paving composite of claim 1, wherein thepolymeric carrier substrate comprises at least one of the groupconsisting of polyethylene, polypropylene, polyethylene andpolypropylene copolymer, polyvinyl chloride, polyamide, acrylic,polyester, thermo plastic polyolefin and ethylene vinyl acetate.
 7. Thepaving composite of claim 6, wherein the polymeric carrier substratecomprises polyethylene.
 8. The paving composite of claim 1, wherein thesurface layer material comprises at least one of the group consisting ofpolyvinyl chloride, acrylic, polyethylene, polyamide, polypropylene, andethylene vinyl acetate.
 9. A method of paving comprising the steps of:laying the paving composite of claim 1 above an underlying layer ofpaving material; and laying an overlying layer of paving material abovethe paving composite.
 10. The method of claim 9, wherein at least one ofthe underlying layer of paving material and the overlying layer ofpaving material comprises asphalt.
 11. The method of claim 9, whereinthe paving composite is laid over the underlying layer of pavingmaterial without spraying a tack emulsion on the underlying layer, andthe overlying layer of paving material is laid over the paving compositewithout spraying a tack emulsion on the paving composite.
 12. The methodof claim 9, wherein the method further comprises laying a reinforcinglayer over the paving composite before laying the overlying layer ofpaving material.
 13. The method of claim 12, wherein the reinforcinglayer comprises a grid of glass fiber strands.
 14. The method of claim9, wherein the method further comprises providing the paving compositein a roll, and the step of laying the paving composite includesunrolling the paving composite over the underlying layer of pavingmaterial.
 15. A paving composite comprising: a polymeric carriersubstrate having first and second major surfaces, wherein the polymericcarrier substrate comprises polyethylene, ethylene vinyl acetate, or acombination thereof; and a surface layer material disposed on the firstand second major surfaces of the polymeric carrier substrate, thesurface layer material comprising ethylene vinyl acetate; wherein thesurface layer material of the paving composite is configured to bond anunderlying layer of paving material to an overlying layer of pavingmaterial, and wherein the surface layer material of the paving compositeis not tacky at a temperature of about 20° C. and a pressure of aboutone atmosphere.
 16. The paving composite of claim 15, wherein thepolymeric carrier substrate comprises low density polyethylene, ethylenevinyl acetate, or a combination thereof.
 17. A paving film comprisingpolyvinyl chloride acrylic latex, wherein the paving film is configuredto bond an underlying layer of paving material to an overlying layer ofpaving material, and wherein the paving film is not tacky at atemperature of about 20° C. and a pressure of about one atmosphere. 18.The paving film of claim 17, wherein the paving film further comprisesabout 1-8 wt. % wax release agent.
 19. The paving film of claim 17,wherein the paving film further comprises about 0-10 wt. % of one ormore of the group consisting of: soluble polymer, ammonia, thickener,colorant, defoamer, and plasticizer.
 20. The paving film of claim 17,wherein the paving film, based upon the weight of dry ingredients,further comprises: 40-60 wt % PVC-acrylic latex; 0-20 wt % internallyplasticized PVC latex; 5-25 wt % styrene-acrylic acid latex; 5-25 wt %ethylene-acrylic acid latex; 0-1 wt % organic oil/silica defoamer; 0-5wt % carbon black dispersion; 0-5 wt % ethylene bis-stearamide (EBS)anti-blocking wax dispersion; 0-10 wt % acrylic solution polymer; 0-2 wt% non-ionic surfactant; 0-1 wt % fluorosurfactant; and 0-5 wt %polyacrylic acid thickener.